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CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing
View ORCID ProfileRyan L. Collins, Matthew R. Stone, Harrison Brand, Joseph T. Glessner, Michael E. Talkowski
doi: https://doi.org/10.1101/049536
Ryan L. Collins
1Psychiatric and Neurodevelopmental Genetics Unit and Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA,
Matthew R. Stone
1Psychiatric and Neurodevelopmental Genetics Unit and Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA,
Harrison Brand
1Psychiatric and Neurodevelopmental Genetics Unit and Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA,
2Department of Neurology, Harvard Medical School, Boston, MA 02114, USA,
Joseph T. Glessner
1Psychiatric and Neurodevelopmental Genetics Unit and Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA,
2Department of Neurology, Harvard Medical School, Boston, MA 02114, USA,
Michael E. Talkowski
1Psychiatric and Neurodevelopmental Genetics Unit and Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA,
2Department of Neurology, Harvard Medical School, Boston, MA 02114, USA,
3Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02141, USA
Article usage
Posted April 20, 2016.
CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing
Ryan L. Collins, Matthew R. Stone, Harrison Brand, Joseph T. Glessner, Michael E. Talkowski
bioRxiv 049536; doi: https://doi.org/10.1101/049536
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